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- References [5]
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- Product number
- ABIN188687 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Forkhead Box P2 (FOXP2) (Isoform 1) antibody
- Antibody type
- Polyclonal
- Description
- Immunogen affinity purified
- Reactivity
- Human, Mouse, Rat
- Host
- Goat
- Epitope
- Isoform 1
- Vial size
- 0.1 mg
- Storage
- Store at -20°C. Avoid freeze-thaw cycles.
- Handling
- Avoid freeze-thaw cycles
Submitted references Expression of Kv1.3 potassium channels regulates density of cortical interneurons.
Renshaw cell interneuron specialization is controlled by a temporally restricted transcription factor program.
Foxp2 inhibits Nkx2.1-mediated transcription of SP-C via interactions with the Nkx2.1 homeodomain.
A differential developmental pattern of spinal interneuron apoptosis during synaptogenesis: insights from genetic analyses of the protocadherin-gamma gene cluster.
A forkhead-domain gene is mutated in a severe speech and language disorder.
Duque A, Gazula VR, Kaczmarek LK
Developmental neurobiology 2013 Nov;73(11):841-55
Developmental neurobiology 2013 Nov;73(11):841-55
Renshaw cell interneuron specialization is controlled by a temporally restricted transcription factor program.
Stam FJ, Hendricks TJ, Zhang J, Geiman EJ, Francius C, Labosky PA, Clotman F, Goulding M
Development (Cambridge, England) 2012 Jan;139(1):179-90
Development (Cambridge, England) 2012 Jan;139(1):179-90
Foxp2 inhibits Nkx2.1-mediated transcription of SP-C via interactions with the Nkx2.1 homeodomain.
Zhou B, Zhong Q, Minoo P, Li C, Ann DK, Frenkel B, Morrisey EE, Crandall ED, Borok Z
American journal of respiratory cell and molecular biology 2008 Jun;38(6):750-8
American journal of respiratory cell and molecular biology 2008 Jun;38(6):750-8
A differential developmental pattern of spinal interneuron apoptosis during synaptogenesis: insights from genetic analyses of the protocadherin-gamma gene cluster.
Prasad T, Wang X, Gray PA, Weiner JA
Development (Cambridge, England) 2008 Dec;135(24):4153-64
Development (Cambridge, England) 2008 Dec;135(24):4153-64
A forkhead-domain gene is mutated in a severe speech and language disorder.
Lai CS, Fisher SE, Hurst JA, Vargha-Khadem F, Monaco AP
Nature 2001 Oct 4;413(6855):519-23
Nature 2001 Oct 4;413(6855):519-23
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- Submitted by
- antibodies-online (provider)
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- Experimental details
- WB
- Submitted by
- antibodies-online (provider)
- Main image
- Experimental details
- WB
Supportive validation
- Submitted by
- antibodies-online (provider)
- Main image
- Experimental details
- IHC
